EU/3/02/109 - orphan designation for treatment of ovarian cancer

oregovomab
OrphanHuman

Overview

On 30 July 2002, orphan designation (EU/3/02/109) was granted by the European Commission to Dorian Regulatory Affairs, The Netherlands, for oregovomab for the treatment of ovarian cancer.
The sponsorship was transferred to ViRexx International Corp. Limited, Ireland, in May 2007.

Tumours that begin in the ovaries are known as ovarian tumours. Ovarian tumours which have potential to grow rapidly and infiltrate surrounding healthy tissues are called ovarian cancers. Due to the absence of symptoms in early stages of the disease the majority of the patients are diagnosed when the tumours have spread locally or to distant parts of the body and cannot be entirely removed. Ovarian cancer is a life-threatening condition.

Several anticancer medicinal products were authorised for the condition in the Community at the time of submission of the application for orphan designation. Although a significant percentage of patients respond to the initial chemotherapy, most ovarian cancers grow again and respond moderately or poorly to subsequent chemotherapy. Satisfactory argumentation has been submitted by the sponsor to justify the assumption that oregovomab might be of potential significant benefit for the treatment of ovarian cancer, particularly based on the novel mechanism of action.

According to the information provided by the sponsor, ovarian cancer was considered to affect about 86,000 persons in the European Union.

*Disclaimer: The number of patients affected by the condition is estimated and assessed for the purpose of the designation, for a European Community population of 377,000,000 (Eurostat 2001) and may differ from the true number of patients affected by the condition. This estimate is based on available information and calculations presented by the sponsor at the time of the application.

Oregovomab is an antibody, which is a protein used by the immune system of the body. Oregovomab binds to a protein released by ovarian cancer tissue. This binding stimulates an immune response of the organism against the cancer cells, which might cause the immune system to recognise and kill cancer cells.

At the time of submission of the application for orphan designation, clinical trials in patients with ovarian cancer were ongoing.

Oregovomab has been designated as an orphan medicinal product in the United States for treatment of ovarian cancers and had not been marketed anywhere worldwide for ovarian cancer, at the time of submission.

According to Regulation (EC) No 141/2000 of 16 December 1999, the Committee for Orphan Medicinal Products (COMP) adopted on 27 June 2002 a positive opinion recommending the grant of the above mentioned designation.

  • the seriousness of the condition,
  • the existence or not of alternative methods of diagnosis, prevention or treatment and
  • either the rarity of the condition (considered to be affecting not more than five in ten thousand persons in the Community) or the insufficient return of development investments.

Designated orphan medicinal products are still investigational products, which have been considered for designation on the basis of potential activity. An orphan designation is not a marketing authorisation. As a consequence, demonstration of the quality, safety and efficacy will be necessary before this product can be granted a marketing authorisation.

Key facts

Active substance
oregovomab
Intended use
Treatment of ovarian cancer
Orphan designation status
Positive
EU designation number
EU/3/02/109
Date of designation
Sponsor

ViRexx International Corp. Limited
No. 1 Main Street
Blessington
County Wicklow
Ireland
Telephone: + 353 1 490 55 57
Telefax: + 353 1 490 62 00
E-mail: information@virexx.com

EMA list of opinions on orphan medicinal product designation

EMA publishes information on orphan medicinal product designation adopted by the Committee for Orphan Medicinal Products (COMP) on the IRIS online platform:

Patients' organisations

For contact details of patients’ organisations whose activities are targeted at rare diseases, see:

  • Orphanet, a database containing information on rare diseases, which includes a directory of patients’ organisations registered in Europe.

  • European Organisation for Rare Diseases (EURORDIS), a non-governmental alliance of patient organisations and individuals active in the field of rare diseases.

EU register of orphan medicines

The list of medicines that have received an orphan designation in the EU is available on the European Commission's website:

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